651724-25-3Relevant articles and documents
Parallel Synthesis of New β2-Amino Esters via Conjugate Nucleophilic Additions
Huck, Jacques,Duru, Christiane,Roumestant, Marie Louise,Martinez, Jean
, p. 2165 - 2168 (2003)
The Michael addition of secondary cyclic aromatic and nonaromatic amines to methyl 2-{[(tert-butoxycarbonyl)amino]methyl}acrylate afforded substituted β2-amino esters in good to excellent yields.
Synthesis of enantiopure β2-homoalanine derivatives via rhodium catalyzed asymmetric hydrogenation
Luehr, Susan,Holz, Jens,Zayas, Odalys,Seidelmann, Oliver,Domke, Lutz,Boerner, Armin
, p. 395 - 401 (2013/06/27)
The stereoselective synthesis of chiral β2-homoalanine derivatives with 99% ee by the Rh-catalyzed enantioselective hydrogenation of prochiral 2-aminomethyl acrylates is described. The subsequent transformation to chiral 3-amino-2-methylpropanols is also demonstrated.